| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.90088606C>A | CA16602461 | IDH2 | c.515G>T (p.Arg172Met) c.359G>T (p.Arg120Met) c.208-104G>T (n.208-104G>T) c.*140G>T (n.*140G>T) c.125G>T (p.Arg42Met) | ClinVar dbSNP COSMIC |
| 15 | g.90088606C>T | CA16602462 | IDH2 | c.515G>A (p.Arg172Lys) c.359G>A (p.Arg120Lys) c.208-104G>A (n.208-104G>A) c.*140G>A (n.*140G>A) c.125G>A (p.Arg42Lys) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.90088606C>G | CA393802239 | IDH2 | c.515G>C (p.Arg172Thr) c.359G>C (p.Arg120Thr) c.208-104G>C (n.208-104G>C) c.*140G>C (n.*140G>C) c.125G>C (p.Arg42Thr) | dbSNP COSMIC |